Certain dioxopiprazinyl-alkyl-phenols

ABSTRACT

3,5-dialkyl-4-hydroxyphenylalkyl substituted piperazine diones are stabilizers for synthetic polymeric materials normally subject to deterioration caused by ultraviolet light. The compounds are prepared by the alkylation reaction between a substituted piperazine dione and 3,5-dialkyl-4-hydroxyphenylalkyl halide. Polymeric compositions containing these stabilizers may also contain a hindered phenolic compound. A typical embodiment is 15-(3&#39;&#39;,5&#39;&#39;-di-t-butyl-4&#39;&#39;-hydroxybenzyl)(7,15diazadispiro(5,1,5,3)hexadecane -14,16-dione).

United States Patent [191 Ramey et a1.

1 1 CERTAIN DIOXOPIPRAZINYL-ALKYL-PHENOLS [751 inventors: Chester E. Ramey, Spring Valley;

John J. Luzzi, Carmel, both of N.Y.

[73] Assignee: Ciba-Geigy Corporation, Ardsley,

[221 Filed: July 12. 1973 Appl. No: 378,472

Related US. Application Data [63] Continuution-in-part of Ser, No. 237.981. March 24,

I972. abandoned.

[52] U.S. CIMH. 260/268 TR; 204/158; 260/458 N; 260/268 DK [51] Int. Cl. C07D 241/00 [58] Field of Search... 260/268 UK, 268 R, 268 TR, 260/268 PC, 268 B1 [56] References Cited UNlTED STATES PATENTS 3.196.153 7/1965 Dazzi 1. 260/268 DK 3118312 11/1965 Orloff 260/268 R 3.318.876 511967 Cignarella et a1 260/240 3529.645 7/1967 Childers .4 260/336 1 Nov. 11, 1975 1549396 12/1970 Dictz v 1 l i 1 1 1 106/300 OTHER PUBLICATIONS Yoshioka, Bull. Chem. Soc, Japan 45(6),

Dwynstee Reel. Trav. Chim. Pays-B215 I968 87(9), 945-956.

Sudo et 211., Bull. Chem. Soc. Japan, 36(1), 34-37 (1963).

Primary E.\'mrzinerR. Gallagher Attorney, Agent, or FirmCharles W, Vanccek 7 Claims, No Drawings CERTAIN DIOXOPIPRAZINYL-ALKYL-PHENOLS RELATED APPLICATION This application is a continuation-in-part of co-pending application Ser. No. 237,98l, filed Mar. 24, 1972, now abandoned.

BACKGROUND OF THE INVENTION This invention relates to the stabilization of organic material normally tending to deteriorate. in particular, the invention relates to the protection of synthetic polymers against the harmful degradative effects, such as discoloration and embrittlement caused by exposure to light, especially ultraviolet light.

It is known that actinic radiation, particularly in the near ultraviolet region, has a deleterious effect on both the appearance and properties of organic polymers. For example, normally colorless or light colored polyesters yellow on exposure to sunlight as do such cellulosics as cellulose acetate. Polystyrene discolors and cracks, with accompanying loss of its desirable physical properties when exposed to actinic light, while vinyl resins, such as polyvinyl chloride and polyvinyl acetate spot and degrade. The rate of air oxidation of polyolefins such as polyethylene and polypropylene is materially accelerated by ultraviolet light.

It has been proposed to stabilize polymeric materials against ultraviolet light deterioration by the use of various types of ultraviolet absorbers. Thus, U.S. Pat. No. 3,004,896 discloses for this purpose 2(2-hydroxyphenylbenzotriazole derivatives, while U.S. Pat. No. 3,189,630 discloses certain metal salts of hydroxybenzoic acids which are useful as actinic stabilizers in synthetic polymers.

DETAILED DISCLOSURE The present invention is directed to a class of ultraviolet light stabilizers which consist of a compound of the formula R and R are independently of each other methyl or ethyl or together with the carbon to which they are bound form a cyclopentyl or cyclohexyl ring, which is unsubstituted or substituted with a methyl group;

n is an integer of from I to 4, and

each of R and R is the same or different (lower)alkyl group containing from i to 8 carbon atoms wherein at least one said alkyl group is branched on the a carbon atom.

By the term alkyl as represented by R and R is intended methyl or ethyl, with methyl being the preferred substituent. Representative of the cycloalkyl groups, as represented by R and R are cyclohexyl, cyclopentyl, Z-methyl, 3-methyl and 4-methylcyclohexyl, and 2- methyl and B-methylcyclopentyl. The preferred cyclo alkyl groups are cyclohexyl and Z-methylcyclohexyl.

Each of the groups R" and R" is the same or different (lower)alkyl group of from 1 to 8 carbon atoms, wherein at least ony of said alkyl groups is branched on the or carbon atom, i.e., methyl, ethyl, n-propyl, isopropyl, n-butyl, secondary butyl, tertiary butyl. t-amyl, thexyl, t-octyl and the like. The preferred groups are tertiary butyl, t-amyl, t-hexyl and t-octyl. The most preferred group is t-butyl.

The invention also relates to compositions of matter which are stabilized against ultraviolet light deterioration which comprises a synthetic organic polymer normally subject to ultraviolet deterioration containing from about 0.005 to 57( by weight of the polymer of the compounds of formula I and preferably from 0.015 to 2% by weight.

The 3,5-dialkyl-4-hydroxyphenylalkyl substituted pi perazine dione derivatives as represented by formula I can be used in combination with other light stabilizers such as 2-(Z-hydroxyphenyl)benzotriazoles, 2-hydroxybenzophenones, nickel complexes and benzoates.

The stabilizers of this invention are suitable for the protection of many synthetic polymers from the deleterious effects of light. Homopolymers, copolymers, and mixtures thereof are embraced within the scope of substrates which may be stabilized with the stabilizers of this invention, along which may be mentioned, polystyrene and including homopolystyrene and copolymers with acrylonitrile and/or butadiene; vinyl resins formed from the polymerization of vinyl halides or from copolymerization of vinyl halides with unsaturated polymerizable compounds, for example, vinyl esters, afiunsaturated acids, afi-unsaturated esters, and unsaturated hydrocarbons such as butadienes and styrene, poly-a'olefins such as high and low density polyethylene, cross-linked polyethylene, polypropylene. poly(4- methyl-pentene-l polybutene-l, and the like including copolymers of poly-oz-olefins such as ethylene-propylene copolymers, and the like; polybutadiene; polyisoprene', polyurethanes such as are prepared from polyols and organic polyisocyanate; polyamides such as hexamethylene-adipamide; polyesters such as polymethyleneterephthalates; polycarbonates such as those prepared from bisphenol-A and phosgene; polyacetals; polyethylene oxide; and polyacrylics such as polyacrylonitrile; polyphenyleneoxides such as those prepared from 2,6-dimethylphenol and the like. Particularly preferred polymers for the compositions of this invention are those normally solid polymers of alpha-olefins having up to 3 carbon atoms, e.g., ethylene-propylene and their copolymers.

The stabilized polymers of the present invention have utility in the normal uses for which plastics are employed and particularly useful for film and fiber. Compounds of this invention may be incorporated in the polymeric substance during the usual processing operations, for example, by hot milling, the composition then being extruded, pressed, blow molded or the like into films, fibers, filaments, hollow spheres and the like. Where the polymer is prepared from a liquid monomer as in the case of styrene, the stabilizer may be dispersed or dissolved in the monomer prior to polymerization or curing.

The compounds of this invention, in addition to their ability to stabilize synthetic polymers against ultraviolet light are also effective in protecting the synthetic poly mers against thermal and oxidative degradation, especially when used in conjunction with 0.01 to 5% by 3 weight of polymer of a sulfur compound such dilaurylthiodipropionate and distearylthiodipropionate.

In addition to the actinic stabilizers described. the plastic compositions may contain other additives such plasticizers. pigments, fillers. dyes. glass or other f1- bers. thermal antioxidants. and the like. For example in most applications. it is desirable to incorporate into the resin composition. sufficient thermal antioxidants to protect the plastic against thermal and oxidative degradation. The amount of antioxidant required will be comparable to that of the actinic stabilizer. Namely. from about 0.005 to and preferably from 0.01 to 2% by weight. Representative of such antioxidants are phosphite esters. such as triphenylphosphite and dibutylphosphite and alkyl arylphosphites such as dibutylphenylphosphite. and the like.

The best results are obtained with the preferred class of thermal antioxidants, the hindered phenols. These compounds have been found to provide the best thermal stabilization with the least discoloration in the compositions of the invention. Typical of these phenolic antioxidants include the following:

I. Phenolic compounds having the general formula Illustrative examples of the compounds shown above are 2.6-di-t-butyl-p-cresol 2-methyl-4.o-di-t-butylphenol and the like. 3. Phenolic compounds having the formula a-( 3 .5-di-t-butyl-4-hydroxybenzyl Q CH'HZN Q 2.2 '-methylene bis( 6-t-butyl-4-mcthylphenol) 2.2'-methylene bis( 6-t-butyl-4-ethylphenol) 4.4'-butylidene-bis( 2 .o-di-t-butylphenol) 4.4'-( Z-butylidene )-bis( Zt-butyl-5-methylphenol) 2.2 '-methylene-bis[ 6-( l-methyleyclohexyl )-4- methylphenol] and the like. (4) Phenolic compounds having the formula Illustrative examples of such compounds are 2,5-di-t-butylhydroquinone 2.o-di-t-butylhydroquinone 2,5-di-t-butyl4-hydroxyanisole 5. Phenolic compounds having the formula QSQ Illustrative examples of such compounds are 4.4 -thiobis-( Z-t-butyl-S-methylphenol) 4.4'-thiobis-( 2 t-butyl-6-methylphenol) 2.2'-thiobis-( 6-t-butyl-4-methylphenol) 6. Phenolic compounds having the formula Illustrative examples of such compounds are octadecyl-( 3.S-dimethyl4-hydroxybenzy'lthio )acetate dodecyl-( 3,5-di-t butyl-4-hydroxybenzylthio )propionate 7. Phenolic compounds having the formula wherein T is hydrogen R or O as defined above.

Illustrative examples of such compounds are l .l.3-tris( 3.S-dimethyl-4-hydroxyphenyl )-propane l .1 .3-tris(5-t-butyl-4-hydroxy-Z-methylphenyl)butane l. l .5 ,5 -tetrakis-( 3 '-t-butyl 4'-hydroxy-6'-methyl phenyl )-n-pentane 8. Phenolic compounds having the formula QCH2 an 282 CH 3 CH 2B3 wherein B. B and B are hydrogen. methyl or Q. provided that when B and B are Q then B is hydrogen or methyl and when I? is Q then B and B are hydrogen or methyl.

Illustrative examples of such compounds are l.4-di( 3 .5-di-t-butyl-4-hydroxybenzyl )-2.3.5,6-tetramethylbenzene 7 2-( 2-stearoyloxyethylthio )ethyl hydroxybenzoate 2-( Z-hydroxyethylthio )ethyl 7-( 3-methyl-5-t-butyL4- hydroxyphenyl )heptanoate 2-( 2-stearoyloxyethylthio )ethyl 7-( 3-methyl-5-tbutyl 4-hydroxyphenyl )heptanoate Sub-class lll 3.5-di-t-butyl-4- LZ-propylene glycol bis-l3-(3,S-di-t-butyl-4-hydroxl Sorbitol hexa-[ 3-( 3,5-di-t-butyl-4-hydroxyphenyl propionate l,2,3-butanetriol tris-[ 3-( 3,5-di-t-butyl-4-hydroxyphenyl )p ropionate] Z-hydroxyethyl 7-( 3 -methyl-5-t-butyl-4-hydroxyphenyl )heptanoate Z-stearoyloxyethyl 7-(3-methyl-5-t-butyl-4-hydroxphenyl)heptanoate LG-n-hexanediol-bisfl 3 ',5 '-di-t-butyl-4-hydroxyphenyl )propionate] The above phenolic ester stabilizers of sub-classes I II and III are more fully described in US. Pat. Nos. 3.330.859, and 3 644,482, respectively.

12. Phenolic compounds having the formula 0 l Q-[CHm-P-OR" where is an integer of l or 2.

Illustrative examples of such compounds are Di-n-octadecyl 3.S-di-t-butyl-4-hydroxybenzylphosphonate Di-n-octadecyl 3-t-butyl-4-hydroxy-5-methylbenzylphosphonate Di-n-octadecyl l-( 3,5-di-t-butyl-4-hydroxyphenyl ethanephosphonate Di-n-tetradecyl 3.5-di-t-butyl-4-hydroxybenzylphosphonate Di-n-hexadecyl 3.5-di-t-butyl4-hydroxybenzylphosphonate Di-n-docosyl-3,S-di-t-butyl-4-hydroxybenzylphosphonate Di-n-octadecyl 3,Sdi-t-butyl-4-hydroxybenzylphosphonate The above di-(higher)alkyl phenolic phosphonates are more fully described in US. Pat. No. 3,281,505.

13. Phenolic compounds having the formula tcn mo Q HH e N- (CH WQ wherein W and Q are defined above.

Illustrative examples of such compounds are:

tris-( 3,5-di-t-butyl-4-hydroxybenzyl )isocyanurate tris-( 3-t-butyl-4-hydroxy-S-methylbenzyl )isocyanurate The above hydroxyphenylalkenyl isocyanurates are more fully described in US. Pat. No. 3,53l,483.

The above phenolic hydrocarbon stabilizers are known and many are commercially available.

While any of the above mentioned antioxidants can be useful in combination with the ultraviolet light stabi lizers of this invention. the preferred antioxidants consist of the hindered phenols in groups 1. 8, 9, l0, 1 1, l2 and 13 as mentioned above. The most preferred hin- R clered phenols are those of groups I, 9, l1, l2 and I3.

The compounds of formula I may be prepared by reacting a substituted piperazine dione of the formula wherein R and R are as defined above. with a 2,6- dialkylsubstituted hydroxyphenylalkylhalide of the formula III wherein R and R are as defined above and X is bromine. chlorine or iodine.

The alkylation reaction is carried out by first preparing the alkali or alkaline earth metal salt of the compound of formula II and reacting the resulting salt with the appropriate organic halide of formula lll in a solvent such as dimethylformamide, isopropanol. or acetone at about C.

The alternative procedure in preparing the compounds of formula I wherein n is equal to l is to react the compound of formula ll with a 2,6-dialkyl-4-dimethylaminophenol in a solvent such as dimethylformam' ide at C.

Compounds of formula 11. wherein R and R form a mono-cyclic ring with the carbon to which they are attached. may be prepared by the self condensation of a cycloalkyl amino cyanohydrin according to the procedure described by R. Sudo and S. lchihera, Bull. Chem. Soc. Japan 36 34 1963) and subsequent hydrolysis as described by E. F. .l. Duynstee et al Recueil de Chemie des Pays Bas 87 945 i968). The cycloalkylamino cyanohydrin is formed by the sequential addition of hydrogen cyanide and ammonia to a cycloalkanone as described by W. E. Noland, R. J. Sundberg and M. L. Michaelson, J. Org. Chem. 28 3576 1963). Although the above references deal specifically with the cycloalkyl case, the procedures therein have been found to be op erable in the alkyl case as well, for example substitution of an alkanone such as acetone for the cycloalkanone such as cyclohexanone in the above procedure.

The following examples, presented for illustration and not limitation, will further serve to typify the nature of the present invention.

EXAMPLE I l-Aminocyclohexanecarbonitrile In a 200 ml 3-necked flask equipped with a stirrer, thermometer, condenser dyring tube and gas inlet tube were placed l g. (0.8 moles) of cyclohexanone cyanohydrin and the reaction mixture was cooled with an ice bath to C. Gaseous anhydrous ammonia was introduced to the reaction mixture through the gas inlet tube for 6 hours. The reaction was then stoppered and allowed to stand overnight.

The next day anhydrous ammonia was again passed through the reaction mixture for 5 hours at C then dry N, was passed through the reaction mixture to entrain any excess NH;,. The product was then dissolved in 250 ml of benzene, the benzene solution washed two times with 250 ml of water, and the solution dried over anhydrous Na SO Evaporation of the benzene yielded the product which was a slightly yellow oil.

In a similar manner, l-aminoisobutyronitrile was prepared by substituting for cyclohexanone cyanohydrin an equivalent amount of acetone cyanohydrin.

Similarly, 1-amino-2-methyl-cyclohexanecarbonitrile is prepared by substituting for cyclohexanone cyanohydrin an equivalent amount of 2-methyl-cyclohexanone cyanohydrin.

EXAMPLE 2 Bis-( l -cyanocyclohexy1)amine In a l-necked round bottomed flask equipped with a capillary nitrogen inlet and an air condenser was placed 48.2 g. (0.39 moles) of l-aminicyclohexane carb0nitrile. The re action mixture was heated in an oil bath to a bath temperature of 75-l00 over 1 hour and placed under a vacuum of using a water aspirator. The reaction was continued for 24 hours, cooled to room temperature, the vacuum released, and the crystalline mass was triturated with ether and filtered by suction, yielding 19.1 g. of white crystals, m.p. l33138C.

In a similar manner, bis( l-cyanoisopropylamine) was prepared by substituting for l-aminocyclohexane carbonitrile an equivalent amount of l-aminoisobutyronitrile.

Similarly, bis-( l-cyano-2-methylcyc1ohexyl)amine is prepared by substituting for l-aminocyclohexanecarbonitrile an equivalent amount of l-amino-Z-methyl cyclohexanecarbonitrile.

EXAMPLE 3 7,l5-diazadispiro[5,l ,5,3]hexadecanel4,16-dione To 406 g. of 96% H 50 contained in a 500 ml 3- necked flask equipped with a stirrer, thermometer and powder funnel was added with stirring and cooling, 30.0 g of powdered bis-( l-cyanocyclohexyl )amine over about a 2 hour period. The temperature of the reaction mixture was maintained at O5 during the addition by using an ice bath. The reaction mixture was allowed to warm to room temperature and to stir overnight. The reaction mixture was then heated to l00C for l hour, then cooled to approximately l5C and poured onto 3000 g. of ice. The aqueous mixture was neutralized to pH 7 by the addition of approximately 800 ml of ION NaOH. The resulting precipitate was collected by suction filtration, washed well with water, and dried in a vacuum oven, yielding a white powder, m.p. 155l60C.

In a similar manner, 2,2,6,6tetramethyl-3,5- diketopiperazine was prepared by substituting for bis( l-cyanohexyl)amine an equivalent amount of bis( 1 -cyanisopropylamine Similarly, 1,9-dimethyl'7, l 5-diazadispiro[ 5, l ,5 ,3- lhexadecane-l4,l6-dione is prepared by substituting for bis-( l-cyanocyclohexyl)amine an equivalent amount of bis-( l-cyano-2-methylcyclohexyl)amine.

EXAMPLE 4 15-( 3',5 '-di-t-butyl-4'hydroxybenzyl-7, l 5-diazadispiro[ 5, l ,5,3]hexadecanel 4, l6-dione In a 200 ml 3-necked flask equipped with a stirrer, thermometer, condenser, drying tube and N inlet was placed a solution of 6.3g (0.025 moles) of 7,15- diazadispiro[ 5, l ,5,3 ]he xadecane l 4, l 6-dione and 6.9g (0.0263 moles) of 2,6-di-t-butyl-4-hydroxybenzyldimethylamine in l00 ml of dimethyl formamide. The reaction flask was heated slowly to C with stirring under N, by an oil bath. The reaction mixture was maintained at 125C for 28 hours and then cooled to room temperature. The reaction mixture was taken up in 300 ml of ether and washed four times with l00 ml of water. To the ether solution was added 50 ml of concentrated HCI affording a precipitate which was filtered with suction. The product was taken up in water and NaOH added until the solution was basic. The water solution was extracted with ether, the ether extracts combined and dried over anhydrous Na SO The ether solution was evaporated, yielding light yellow crystalline material, which was recrystallized from heptane giving white crystals, mp. 122l25C.

By following the above procedure, and substituting for 7, l5-diazadispiro[ 5 ,1,5,3]hexadecane-14,16-dione an equivalent amount of:

a. 2,2,6,6-tetramethyl-3,S-diketopiperazine b. l ,9-dimethyl-7, 15 -diazadispiro[ 5, l ,5,3 ]hexadecane-14,16-dione there is respectively obtained the following compounds ramethyl-3,S-diketopiperazine; m.p. 1 18l 2 1C dimethyl-7,1S-diazadispirolS,1,5,3]hexadecane- 14,16-dione.

EXAMPLE 5 15-( 3 ,5 '-Di-T-Butyl-4 '-hydroxybenzyl )7, l S-diazadispiro[5,l ,S,3]hexadecane-15, l6-dione To a solution of l0.0g (0.04 moles) of 7.15 diazadispiro[S,1,5,3]hexadecane-l4,l6-dione in l50 ml of anhydrous methanol in a 500 ml flask is added 2.6g of 86% KOH (0.04 moles) and the mixture is shaken until solution is obtained. The reaction mixture is evaporated to dryness under reduced pressure. The residue is transferred to a 300 ml 3-necked flask equipped with a 1 l stirrer. thermometer, condenser with drying tube. dropping funnel and nitrogen inlet tube with the aid of a small amount of dry DMF. To the potassium imide salt, under a nitrogen atmosphere. is added 150 ml of dry DMF. To the stirred solution is added dropwise a solution of 102g (0.04 moles) of 3.5-di-t-butyl-4 hydroxybenzyl chloride in 50 ml of dry DMF. The reaction mixture is heated to 75C for 3 hours, then cooled and allowed to stir at room temperature for l6 hours. The reaction mixture is taken up in 500 ml of ether and washed with water. To the ether solution is added 50 ml of concentrated HCl affording a precipitate which is collected by suction filtration. The product is taken up in water and NaOH added until the solution is basic. The water solution is extracted with ether, the ether extracts combined and dried over anhydrous Na SO The ether solution is evaporated yielding the product which is recrystallized from heptane.

By essentially following the above procedure, and substituting for the reactants used. i.e.. 7,l-diazadispiro[5 l ,5,3 lhexadecanel 4. l 6-dione and 3,5-di-tbutyl-4-hydroxybenzyl chloride, an equivalent amount of the following reactants:

a. 7. l 5-diazadispiro[ 5, l ,5,3 ]hexadecanel 4, l 6- dione 3-t-butyl-5-methyl-4-hydroxybenzyl chloride b. 7, l S-diazadispirolil ,5,3]hexadecane- 14,16- dione [H3',5'-di-t-butyl-4'-hydroxyphenethyl)- chloride c. 7, l 5-diazadispiro[ 5, l ,5,3 ]hexadecane- [4, l 6

dione 3 (3,5'-di-t-butyl-4"hydroxyphenyl)propyl chloride 7, l 5-diazadispirol5, l ,5,3]hexadecane- 14,16- dione 4( 3',5 '-di-t-butyl-4'-hydroxyphenyl )butyl chloride e. 2,2,6,6-tetramethyl-3.5-diketopiperazine methyl-6-t-octyl-4-hydroxybenzyl chloride f. 7, l 5-diazadispiro[ 5,1 ,5 ,3 ]hexadecanel 4, l 6-dione 3.5-di-t-octyl-4-hydroxybenzyl chloride there is respectively obtained the following compounds:

a. 3 -t-butyl5 'methyl-4' hydroxybenzyl )7, l 5- diazadispiro[5, l ,5,3]hexadecane-14,16-dione 15-134 3 ,5-di-t-butyl-4'-hydroxyphenethyl )7 1 5- diazadispirol 5. l ,5,3]hexadecanel 4, l b-dione m.p. l40-l44 c. 15-( 3'-( 3",5 '-di-t-butyl-4' '-hydroxyphenyl propyl )-7, l 5-dia2adispiro[ 5, l ,5 ,3 ]he xadecanel4,l6dione l5 4'-( 3 ',5' '-di-t-butyl-4"-hydroxyphenyl butyl )-7 ,15-diazadispiro[5,l ,5,3]hexadecane- 14,16-dione) e. 4( 3 '-methyl-5 '-t-octyl-4'-hydroxybenzyl )-2,2,6,6-

tetramethyl-3,5-diketopiperazine f. 15-( 3',5 '-di-t-octyl-4'-hydroxybenzyl )7, l 5- diazadispirol 5, l ,5 ,3 lhexadecane- 14, l 6-dione EXAMPLE 6 Artifical Light Exposure Test Deterioration of most polymers caused by ultraviolet light is so slow at ambient temperatures, even in the absence of stabilizers. that testing of the effects of stabilizers generally must be conducted either at higher temperatures or in an accelerated artificial light exposure device in order to yield results in a convenient period of time. The tests conducted on polymers using an artificial light exposure device is described below:

12 a. Sample Preparation 5 mil Film Unstabilized polypropylene powder (Hercules Profax 650l is thoroughly blended with the indicated amounts of additives. The blended material is then milled on a two roll mill for 5 minutes at 182C. The milled sheet is then compression molded at 220C into 5 mil thick film under a pressure of l psi and water cooled in the press.

b. Testing Method This test is conducted in a FS/BL unit, basically of the American Cyanamid design. which consists of 40 tubes of alternating fluorescent sunlamps and black lights (20 of each). The 5 mil sample film which are mounted on 3 X 2 inch lR card holders with A X 1 inch windows and are placed on a rotating drum 2 inches from the bulbs in the FS/BL unit. The time in hours is noted for the development of 0.5 carbonyl absorbance units are determined on an Infrared Spectrophotometer. The development of carbonyl functional groups in the polymer is proportional to the amount of degradation caused by the ultraviolet light exposure.

The test results reported below were obtained according to the procedures described above. The amounts of the additives are expressed in weight per cent based on the weight of the polymer.

Table 1 Time in Hours to .5 Carbonyl Formulation Absorbance Units hydroxyhenzyl )2,2,6,o-tetramethyl piperazine 3.5-dione 685 (1.59? l5-B-( 3'.5-di-t-butyl-4'- hydroxyphenethyl )7, l S-diazadispiro [5.1.5.3Ihexadecane l4.lb-dione 4-H) Control" 225 The sample tested and the control contains (1.2% of (di'octadecylt 3.5-di-t-hutyl- 4-h \dro.\yhenzyl) phosphnnate hieh is an antioxidant which pre tenLs oxidative degradation of polypropylene during processing.

Other hindered phenolic antioxidants may be used in place of dioctadecyl( 3 ,5-di-t-butyl-4-hydroxybenzyl phosphonate in the above mentioned composition for example, di-n-octadecyl a-(3-t-butyl-4-hydroxy-5- methylbenzyl )malonate 2,4-bis-(n-octylthio )-6-( 3 ,5- di-t-butyl-4-hydroxyanilino)-l ,3,5triazine, octadecyl 3-( 3 ,5 -di-t-butyl-4 -hydroxyphenyl )propionate, pentaethylthritol-tetrakis 3 3 ,5 -di-t-butyl-4-hydroxyphenyl )propionatel tris-( 3,S-di-t-butyl-4-hydroxybenzyl )isocyanurate, respectively.

EXAMPLE 7 a. A composition comprising acrylonitrilebutadienestyrene terpolymer and 1% by weight of l5-(3'-(3",5"- di-t-butyl-4' '-hydroxyphenylpropyl )-7 l S-diazadispiro[ 5,1 ,5 ,31hexadecanel4,l o-dione resists embrittlemerit due to exposure to ultraviolet light longer than one which does not contain the stabilizer.

b. A composition comprising polyurethane prepared from toluene diisocyanate and alkylene polyols and 1.0% by weight of 4(3-methyl-5'-t-octyl-4'-hydroxybenzyl)-2,2,6,6-tetramethyl-3,5-diketopiperazine is more stable to sunlight, under fluorescent sunlamps, black lights and fluorescent lights then the unformulated polyurethane,

c. A composition comprising a polycarbonate prepared from bisphenol-A and phosgene and 1% by weight of 4'-( 3 ",5 '-di-t-butyl-4"-hydroxyphenylbutyl-7, l 5-diazadispiro[ 5 .1 ,5,3 ]hexadec ane- 14, l 6- dione resists discoloration due to exposure to ultraviolet light longer than one which does not contain the sta bilizer.

EXAMPLE 8 a. A stabilized linear polyethylene is prepared by incorporating therein 0.5% by weight of l5-(3',5' di-tbutyl-4-hydroxybenzyl )-7 l 5-diazadispiro[ 5, l ,5,3- ]hexadecane 14,16-dione. The stabilized compositions resist embrittlement due to exposure to ultraviolet light longer than one which does not contain the stabilizer.

b. A stabilized polyamide (nylon 6,6) is prepared by incorporating therein 01% by weight of 4(3,5'-di-tbutyl-4-hydroxybenzyl)-2,2,6,o-tetramethyl-3,5- diketopiperazine. The light stability of the stabilized composition is superior to that of an unstabilized polyamide.

c. A stabilized polyphenylene oxide polymer (prepared by polymerizing 2,6-dimethylphenol) is prepared by incorporating therein 0.5% by weight l5-(3-t-butyl- 5 -methyl-4-hydroxybenzyl )-7, l 5diazadispiro[5,l ,5,3]hexadecane-14,16-dione. The stabilized compositions resist embrittlement due to exposure to ultraviolet light longer than one which does not contain the stabilize r.

d. A stabilized crystalline polystyrene is prepared by incorporating therein 0.1% by weight of l5-/3-( 3',5-dit-butyl-4 '-hydroxyphenethyl )7 l S-diazadispiro[5,l .5,3]hexadecane-14,16-dione. The stabilized compositions resist embrittlement due to exposure to ultraviolet light longer than one which does not contain the stabilize r.

EXAMPLE 9 High impact polystyrene resin containing elastomer (i.e., butadiene-styrene) is stabilized against loss of elongation properties due to exposure to ultraviolet light by incorporation of 0.3% by weight of l5-(3',5'- di-t-octyl-4 -hydroxybenzyl )-7 l 5-diazadispiro[5,l ,5,3]hexadecane-14,16-dione.

The unstabilized resin is dissolved in chloroform and the stabilizer then added, after which the mixture is cast on a glass plate and the solvent evaporated to yield a uniform film which, upon drying, is removed and cut up, and then pressed for 7 minutes at a temperature of 163C and a pressure of 2,000 pounds per square inch into a sheet of uniform thickness mil). The sheets are then cut into strips approximately 4 X 0.5 inches. A portion of these strips is then measured for percent of elongation in the lnstron Tensile Testing Apparatus (lnstron Engineering Corporation, Quincy, Massachusetts). The remaining portion of the strips are placed in an FS/BL chamber according to Example 6 (b) except that the time to 50% reduction in elongation is measured. The stabilized polystyrene resin retains its elongation property longer than the unstabilized resin.

Similar results are obtained when an equivalent amount of the following stabilizers are used in place of the above mentioned stabilizer.

a. 0.1% by weight of 4(3,5'-di-t-butyl-4'-hydroxybenzyl)-2,2.6,6-tetramethyl-3,S-diketopiperazine ybenzyl)-l,9-dimethyl-7,l5-diazadispiro[5.1,5,3- ]hexadecane l 4, l 6-dione 14 c. 0.l% by weight of l5-(3'-t-butyl-5'-methyl-4'- hydroxybenzyl )7, l 5 -diazadispiro[5.1,5,31hexadecane-14,l6-dione d. 0.5% by weight of l5-B-(3,5-di-t-butyl-4-hydroxyphenethyl )7, l S-diazadispirol 5, l ,5 ,3 ]hexadecane- 14,16-dione e. l% by weight of l5-(3'43",5-di-t-butyl-4"- hydroxyphenyhpropyl}-7,l5-diazadispiro[5,1,5 ,3- )hexadecanel 4, l 6-dione f. 0.5% by weight of l5-{4'-(3",5"-di-t-butyl-4"- hydroxyphenyl )butyl} -7, l 5-diazadispiro[ 5. l .5,3- ]hexadecanel 4, l fi-dione g. 0.5% by weight of 4(3-methyl-5'-t-octyl-4- hydroxybenzyl )-2 ,2 ,6,6-tetramethyl-3 .S-diketopiperazine.

Antioxidants may also be incorporated into each of the above mentioned compositions for example. di-noctadecyl-a,a'-bis( 3t-butyl-4-hydroxy-S-methylbenzyl)malonate, 2,4-bis(4hydroxy-3,5-di-t-butylphenoxy)-6-(n-octylthioethylthio)-1.3.5-tria2ine. 2.4-bis( 3,5- di-t-butyl-hydroxyphenoxy )-6-( n-octylthio l ,3,5-tria zine di-n-octadecyl 3,S-di-t-butyl-4-hydroxybenzyl phosphonates and octadecyl 3( 3 ',S '-di-tbutyl-4'- hydroxyphenyl )propionate respectively.

What is claimed is: l. A compound of the formula 2. A compound according to claim 1 having the formula 3. A compound according to claim 2 wherein R and R are tertiary butyl.

4. A compound according to claim 1 which is l5-( 3 5 '-di-t-butyl-4'-hydroxybenzyl )-7, l S-diazadispiro[S, l ,5,3]hexadecane- 14,1 o-dione.

5. A compound according to claim 1 which is l5-( 3'- methyl-S '-t-butyl-4-hydroxybenzyl )-7 .15-diazadispiro{5, l ,5 ,3]hexadecane-14,16-dione. 

1. A COMPOUND OF FORMULA
 2. A compound according to claim 1 having the formula
 3. A compound according to claim 2 wherein R3 and R4 are tertiary butyl.
 4. A compound according to claim 1 which is 15-(3'',5''-di-t-butyl-4''-hydroxybenzyl)-7,15-diazadispiro(5,1,5,3)hexadecane -14, 16-dione.
 5. A compound according to claim 1 which is 15-(3''-methyl-5''-t-butyl-4''-hydroxybenzyl)-7,15 -diazadispiro(5,1,5,3)hexadecane-14, 16-dione.
 6. A compound according to claim 1 which is 15-( Beta -(3'',5''-di-t-butyl-''4-hydroxyphenyl)ethyl)7,15-diazadispiro(5,1,5, 3)hexadecane-14,16-dione.
 7. A compound according to claim 1 which is 15-(3''-(3'''',5''''-di-t-butyl-4''''-hydroxyphenyl)propyl)7,15-diazadispiro(5,1,5, 3)hexadecane-14,16-dione. 